van Welsem M E, Hogenhuis J A, Meininger V, Metsaars W P, Hauw J-J, Seilhean D
Laboratoire de Neuropathologie Raymond Escourolle, Hôpital de la Salpêtrière, 47 Boulevard de l'Hôpital, 75651 Paris Cedex 13, France.
Acta Neuropathol. 2002 Jun;103(6):583-9. doi: 10.1007/s00401-001-0507-3. Epub 2002 Feb 7.
Specific pathological hallmarks have been described in amyotrophic lateral sclerosis (ALS), which include motor neuronal loss, Bunina bodies (BBs) and skein like inclusions (SLIs). We investigated the relation between these three lesions in the cervical and lumbar anterior horns and the hypoglossal nuclei of 20 ALS patients and 9 controls using a quantitative light microscopy study. Immunohistochemistry with anti-cystatin C and anti-ubiquitin was used to detect the BBs and SLIs, respectively. A significant relation between the severity of neuronal loss and the proportion of SLI-containing neurons was found in the spinal cord, whereas no relation was found with BBs. We therefore propose that BBs and SLIs participate in two different steps of the cascade leading to neuronal loss.
肌萎缩侧索硬化症(ALS)具有特定的病理特征,包括运动神经元丧失、布尼纳小体(BBs)和丝状包涵体(SLIs)。我们采用定量光学显微镜研究,调查了20例ALS患者和9例对照者的颈、腰前角及舌下神经核中这三种病变之间的关系。分别使用抗胱抑素C和抗泛素免疫组织化学方法检测BBs和SLIs。在脊髓中发现神经元丧失的严重程度与含SLI神经元的比例之间存在显著关系,而与BBs无相关性。因此,我们提出BBs和SLIs参与了导致神经元丧失的级联反应的两个不同步骤。